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人19型腺病毒:一株角结膜炎分离株的基因组及生物信息学分析

Human adenovirus type 19: genomic and bioinformatics analysis of a keratoconjunctivitis isolate.

作者信息

Robinson Christopher M, Shariati Fatemeh, Zaitshik Jeremy, Gillaspy Allison F, Dyer David W, Chodosh James

机构信息

The Molecular Pathogenesis of Eye Infection Research Center, Dean A. McGee Eye Institute, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

出版信息

Virus Res. 2009 Jan;139(1):122-6. doi: 10.1016/j.virusres.2008.10.001. Epub 2008 Dec 4.

Abstract

Human adenovirus type 19 (HAdV-19) is a major etiologic agent of epidemic keratoconjunctivitis (EKC), a common and severe eye infection associated with long-term visual morbidity due to persistent corneal inflammation. Ironically, while the prototype strain of HAdV-19 does not cause eye infections, other isolates of the serotype have caused major outbreaks of EKC. Here we have sequenced a clinical isolate of HAdV-19 (HAdV-19 strain C) from a human patient with EKC. Global pairwise alignment of HAdV-19C to other HAdV species D serotypes identified areas of sequence divergence in the penton base (host cell internalization signal), hexon (principal viral capsid structural protein), E3 (site of immunomodulatory genes), and fiber (host cell-binding ligand) regions. Comparison of HAdV-19 strain C to the recently sequenced HAdV-37, another EKC causing serotype, identified sequence diversity in the penton base and hexon, but sequence conservation in the E3 and fiber regions. Elucidation of the HAdV-19C genome will facilitate future studies into the pathogenesis of EKC, and may shed light on the genetic determinants of corneal tropism.

摘要

人19型腺病毒(HAdV-19)是流行性角结膜炎(EKC)的主要病原体,EKC是一种常见且严重的眼部感染,因持续性角膜炎症会导致长期视力损害。具有讽刺意味的是,虽然HAdV-19的原型毒株不会引起眼部感染,但该血清型的其他分离株却引发了EKC的大规模暴发。在此,我们对一名EKC患者的HAdV-19临床分离株(HAdV-19毒株C)进行了测序。将HAdV-19C与其他D种血清型腺病毒进行全基因组比对,确定了五聚体基底(宿主细胞内化信号)、六邻体(主要病毒衣壳结构蛋白)、E3区(免疫调节基因位点)和纤维(宿主细胞结合配体)区域的序列差异。将HAdV-19毒株C与最近测序的另一种导致EKC的血清型HAdV-37进行比较,发现五聚体基底和六邻体存在序列多样性,但E3区和纤维区域存在序列保守性。阐明HAdV-19C基因组将有助于未来对EKC发病机制的研究,并可能揭示角膜嗜性的遗传决定因素。

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